Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

P Stromme, ME Mangelsdorf, MA Shaw, Karen Lower, SM Lewis, H Bruyere, V Lutcherath, AK Gedeon, RH Wallace, IE Scheffer, Gillian Turner, Michael Partington, SG Frints, JP Fryns, Grant Sutherland, JC Mulley, Jozef Gecz

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    361 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)441-445
    Number of pages5
    JournalNature Genetics
    Volume30
    Publication statusPublished - 2002

    Cite this

    Stromme, P., Mangelsdorf, ME., Shaw, MA., Lower, K., Lewis, SM., Bruyere, H., Lutcherath, V., Gedeon, AK., Wallace, RH., Scheffer, IE., Turner, G., Partington, M., Frints, SG., Fryns, JP., Sutherland, G., Mulley, JC., & Gecz, J. (2002). Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy. Nature Genetics, 30, 441-445.